multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii
Ask a doctor about a prescription for multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii
How to use multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii
Leaflet attached to the packaging: information for the user
multiBic with potassium 4 mmol/l solution for hemodialysis/hemofiltration
Read the leaflet carefully before using the medicine, as it contains important information for the patient.
- Keep this leaflet, you may need to read it again.
- If you have any further questions, ask your doctor or nurse.
- If you experience any side effects, including any not listed in this leaflet, tell your doctor or nurse. See section 4.
Table of contents of the leaflet:
- 1. What is multiBic with potassium 4 mmol/l and what is it used for
- 2. Important information before using multiBic with potassium 4 mmol/l
- 3. How to use multiBic with potassium 4 mmol/l
- 4. Possible side effects
- 5. How to store multiBic with potassium 4 mmol/l
- 6. Package contents and other information
1. What is multiBic with potassium 4 mmol/l and what is it used for
multiBic with potassium 4 mmol/l is a solution for continuous renal replacement therapy, used to remove waste products from the patient's body. It is used in patients with kidney damage and also in the treatment of poisoning. The type of solution the patient receives depends on the amount of potassium (salt) in the blood. The attending physician will regularly check the patient's potassium levels in the blood.
2. Important information before using multiBic with potassium 4 mmol/l
When not to use multiBic with potassium 4 mmol/l
- if you are hypersensitive to any of the active substances or any of the other ingredients of the medicine (listed in section 6);
- if you have hyperkalemia (high potassium levels in the blood);
- if you have metabolic alkalosis (a condition where there is too much bicarbonate in the blood);
- if it is not possible to achieve sufficient blood flow through the hemofilter (a filter used to filter the blood);
- if there is a high risk of bleeding associated with medications necessary to prevent clotting in the hemofilter.
Warnings and precautions
Before starting treatment with multiBic with potassium 4 mmol/l, discuss it with your doctor.
- Do not use until the solutions in both compartments of the bag are fully mixed.
- Do not use the solution at a temperature lower than room temperature.
- The drainage set used to administer the ready-to-use solution should be checked every 30 minutes. If precipitate (solid sediment) is found in the drainage set, the bag and drainage set should be replaced immediately and the patient should be closely monitored.
- The attending physician will check the patient's hydration status (amount of water in the body), potassium, sodium, and other electrolyte levels, as well as some waste products and sugar levels in the blood. The physician may also provide dietary advice.
Children
There is no established use of multiBic with potassium 4 mmol/l in children.
multiBic with potassium 4 mmol/l and other medicines:
Tell your doctor about all medicines you are taking or have recently taken, as well as any medicines you plan to take.
The following interactions may occur:
- toxic effects of digitalis glycosides (used in heart disease);
- electrolyte supplementation, parenteral nutrition (intravenous nutrition), and other infusion treatments. Their effect on serum levels and fluid status during this treatment should be considered;
- this therapy may decrease the levels of medicinal products in the blood. Dose modification may be required.
Pregnancy and breastfeeding:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor before using this medicine.
There are no data or only limited data on the use of multiBic with potassium 4 mmol/l in pregnancy and breastfeeding.
This medicine should only be used during pregnancy if the doctor considers it necessary.
Breastfeeding is not recommended during treatment with multiBic with potassium 4 mmol/l.
3. How to use multiBic with potassium 4 mmol/l
multiBic with potassium 4 mmol/l is administered in a hospital or other medical facility. The attending physician has the knowledge to administer this medicine.
If you have any doubts, ask your doctor.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Side effects of multiBic with potassium 4 mmol/l:
- nausea
- vomiting
- muscle cramps
- blood pressure changes
Some side effects may be caused by too much or too little fluid in the body. These include:
- shortness of breath
- swelling of the ankles and feet
- dehydration (e.g., dizziness, muscle cramps, thirst)
- blood disorders (e.g., abnormal electrolyte levels in the blood)
The exact frequency of these events is not known (cannot be estimated from the available data).
Reporting suspected side effects
If you experience any side effects, including any not listed in this leaflet, tell your doctor or nurse. Side effects can be reported directly to the "national reporting system" listed in Annex V.*
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will help to gather more information on the safety of this medicine.
5. How to store multiBic with potassium 4 mmol/l
Store the medicine out of sight and reach of children.
Do not store below 4°C.
Storage conditions after mixing the two compartments of the bag:
The ready-to-use solution should not be stored above 30°C and should be used within 48 hours.
Do not use this medicine after the expiry date stated on the label, after the "Expiry date". The expiry date is the last day of the specified month.
6. Package contents and other information
What multiBic with potassium 4 mmol/l contains
- The active substances are: potassium chloride, sodium chloride, sodium bicarbonate, calcium chloride dihydrate, magnesium chloride hexahydrate, and glucose monohydrate.
- Other ingredients of the medicine are: water for injection, hydrochloric acid (25%), carbon dioxide, and sodium dihydrogen phosphate dihydrate.
What multiBic with potassium 4 mmol/l looks like and what the package contains:
multiBic with potassium 4 mmol/l is supplied in a two-compartment bag (two compartments containing different solutions). After mixing the solutions from both compartments, a ready-to-use solution is obtained.
Each bag contains a total of 5000 ml of solution. The ready-to-use solution is clear and colorless.
Each bag is equipped with an HF connector, a Luer lock connector, and an injection port, and is covered with a protective foil.
Package size:
2 bags of 5000 ml
Marketing authorization holder and manufacturer
Marketing authorization holder
Fresenius Medical Care Deutschland GmbH, Else-Kröner-Straße 1,
61352 Bad Homburg v.d.H., Germany
Manufacturer
Fresenius Medical Care Deutschland GmbH, Frankfurter Strasse 6-8, 66606 St. Wendel, Germany
Distributor:
Fresenius Medical Care Polska S.A.
tel.: +48 61 83 92 600
Date of last revision of the leaflet:02/2025
Information intended for healthcare professionals only, see the end of this leaflet.
The following information is intended for healthcare professionals only:
1000 ml of the ready-to-use solution contains:
pH ≈ 7.4
Theoretical osmolality (Osmolar. theor.) 300 mOsm/l
Use only if the ready-to-use solution is clear and colorless, and the bag and connectors are undamaged.
The solution is for single use only. Any unused portion of the solution should be discarded.
Use only with a pump integrated with the extracorporeal blood treatment device.
Instructions for use
The hemodialysis/hemofiltration solution should be administered in three stages:
- 1. Removal of the protective foil and careful inspection of the bag
| Potassium chloride | 0.2982 g |
| Sodium chloride | 6.136 g |
| Sodium bicarbonate | 2.940 g |
| Calcium chloride dihydrate | 0.2205 g |
| Magnesium chloride hexahydrate | 0.1017 g |
| Glucose monohydrate | 1.100 g |
| (Glucose) | (1.000 g) |
| K+ | 4.0 mmol/l |
| Na+ | 140 mmol/l |
| Ca2+ | 1.5 mmol/l |
| Mg2+ | 0.50 mmol/l |
| Cl- | 113 mmol/l |
| HCO3- | 35 mmol/l |
| Glucose | 5.55 mmol/l |
The protective foil should be removed immediately before use. Plastic packaging may occasionally be damaged during transport from the manufacturer to the clinic (dialysis station) or within the clinic itself. This can cause contamination and growth of bacteria and fungi in the solutions. Therefore, the bag should be carefully inspected before mixing. Particular attention should be paid to even the smallest damage to the closure, the weld separating the two compartments, and the corners of the bag, looking for possible contamination.
- 2. Mixing the contents of the two compartments
Both solutions should be mixed immediately before use, resulting in a ready-to-use solution.
A)
B) C)
Unfold the small
compartment.
Roll up the bag with the solution,
starting from the corner
opposite the small
compartment…
…..until the weld between the two compartments
opens along its entire length, and
the solutions from both compartments mix.
After mixing the solutions from both compartments, check that the weld line is completely open, the mixed solution is clear and colorless, and the bag does not leak.
- 3. Using the ready-to-use solution
The ready-to-use solution should be used immediately after mixing or within 48 hours of mixing.
Any additives to the ready-to-use solution can only be introduced after it has been thoroughly mixed. After adding an additive, the ready-to-use solution should be thoroughly mixed again before use.
Additions of sodium chloride solution (up to 30%) or alternatively water for injection are compatible with this medicinal product and may be administered, if necessary, to adjust the sodium concentration to limit the rate of change of sodium concentration in cases of severe hyper- or hyponatremia.
Detailed information is contained in the Summary of Product Characteristics.
Unless otherwise instructed, the ready-to-use solution should be warmed to a temperature of 36.5°C - 38.0°C before use. The exact temperature is determined based on clinical requirements and the equipment used.
- Country of registration
- Prescription requiredNo
- Manufacturer
- ImporterFresenius Medical Care Deutschland GmbH
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
- Alternatives to multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltraciiDosage form: Solution, 9 mg/mlActive substance: sodium chloridePrescription requiredDosage form: Solution, 100 mg/mlActive substance: dextranManufacturer: Fresenius Kabi Italia S.r.L.Prescription not requiredDosage form: Concentrate, -Active substance: electrolytes in combination with other drugsManufacturer: Fresenius Kabi Norge ASPrescription not required
Alternatives to multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii in other countries
The best alternatives with the same active ingredient and therapeutic effect.
Alternative to multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii in Ukraine
Alternative to multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii in Spain
Online doctors for multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii
Discuss dosage, side effects, interactions, contraindications, and prescription renewal for multibic z potasem 4 mmol/l roztvur do hemodializi/do hemofiltracii – subject to medical assessment and local rules.
Get updates and exclusive offers
Be the first to know about new services, marketplace updates, and subscriber-only promos.
